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390 Publikationen

2019 | Zeitschriftenaufsatz | E-Veröff. vor dem Druck | PUB-ID: 2937586
L. Schlotawa, et al., “Severe neonatal multiple sulfatase deficiency presenting with hydrops fetalis in a preterm birth patient.”, JIMD reports, vol. 49, 2019.
PUB | DOI | PubMed | Europe PMC
 
2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2934622
V. Walhorn, et al., “Exploring the Sulfatase 1 Catch Bond Free Energy Landscape using Jarzynski's Equality”, BIOPHYSICAL JOURNAL, vol. 116, Cell Press, 2019, pp.430A-431A.
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2019 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2934113
T. Krüger, T. Dierks, and N. Sewald, “Formylglycine-generating enzymes for site-specific bioconjugation”, BIOLOGICAL CHEMISTRY, vol. 400, 2019, pp. 289-297.
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933913
L. Schlotawa, et al., “Protein disulfide isomerase is a possible target for disease modification in multiple sulfatase deficiency”, MOLECULAR GENETICS AND METABOLISM, MOLECULAR GENETICS AND METABOLISM, vol. 126, San Diego: ACADEMIC PRESS INC ELSEVIER SCIENCE, 2019, pp.S131-S132.
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2019 | Kurzbeitrag Konferenz / Poster | Veröffentlicht | PUB-ID: 2933914
T.O. Silva, et al., “Attenuated multiple sulfatase deficiency: Description of two Brazilian patients showing interesting clinical and genetic findings”, MOLECULAR GENETICS AND METABOLISM, MOLECULAR GENETICS AND METABOLISM, vol. 126, ACADEMIC PRESS INC ELSEVIER SCIENCE, 2019, pp.S135-S136.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920942
T. Krüger, et al., “Two-fold Bioorthogonal Derivatization by Different Formylglycine-Generating Enzymes”, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, vol. 57, 2018, pp. 7245-7249.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2931507
S. Khateb, et al., “A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans”, GENETICS IN MEDICINE, vol. 20, 2018, pp. 1004-1012.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2921018
L. Schlotawa, et al., “Recognition and ER Quality Control of Misfolded Formylglycine-Generating Enzyme by Protein Disulfide Isomerase”, Cell Reports, vol. 24, 2018, pp. 27-37.e4.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2933928
D. Maynard, et al., “The function of the oxylipin 12-oxophytodienoic acid in cell signaling, stress acclimation, and development”, JOURNAL OF EXPERIMENTAL BOTANY, vol. 69, 2018, pp. 5341-5354.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2920271
S. Stroobants, et al., “Sensorimotor and Neurocognitive Dysfunctions Parallel Early Telencephalic Neuropathology in Fucosidosis Mice”, FRONTIERS IN BEHAVIORAL NEUROSCIENCE, vol. 12, 2018, : 15.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2919061
R. Ahrens-Nicklas, et al., “Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement”, MOLECULAR GENETICS AND METABOLISM, vol. 123, 2018, pp. 337-346.
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2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2918283
A. Wieczorek, et al., “Genetically modified human type II collagen for N- and C-terminal covalent tagging”, CANADIAN JOURNAL OF CHEMISTRY, vol. 96, 2018, pp. 204-211.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909071
D. Roy, et al., “Loss of HSulf-1: The Missing Link between Autophagy and Lipid Droplets in Ovarian Cancer”, SCIENTIFIC REPORTS, vol. 7, 2017, : 41977.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2909150
X. Pan, et al., “Mice, double deficient in lysosomal serine carboxypeptidases Scpep1 and Cathepsin A develop the hyperproliferative vesicular corneal dystrophy and hypertrophic skin thickenings”, PLoS One, vol. 12, 2017, : e0172854.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916520
I. Jaszczuk, et al., “Expanding the genetic cause of multiple sulfatase deficiency: A novel SUMF1 variant in a patient displaying a severe late infantile form of the disease”, MOLECULAR GENETICS AND METABOLISM, vol. 121, 2017, pp. 252-258.
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2017 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2908778
O.P. Dhamale, et al., “Arylsulfatase K is the Lysosomal 2-Sulfoglucuronate Sulfatase”, ACS Chemical Biology, vol. 12, 2017, pp. 367-373.
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2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2904124
K. Kruszewski, et al., “Degeneration of Photoreceptor Cells in Arylsulfatase G-Deficient Mice”, INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, vol. 57, 2016, pp. 1120-1131.
PUB | DOI | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2905616
H. Wolf, et al., “A mouse model for fucosidosis recapitulates storage pathology and neurological features of the milder form of the human disease”, Disease Models & Mechanisms, vol. 9, 2016, pp. 1015-1028.
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2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2784664
I. Kalus, et al., “Sulf1 and Sulf2 Differentially Modulate Heparan Sulfate Proteoglycan Sulfation during Postnatal Cerebellum Development: Evidence for Neuroprotective and Neurite Outgrowth Promoting Functions”, PLoS ONE, vol. 10, 2015, : e0139853.
PUB | DOI | WoS | PubMed | Europe PMC
 
2015 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2780450
J. Peng, et al., “Eukaryotic formylglycine-generating enzyme catalyses a monooxygenase type of reaction”, FEBS Journal, vol. 282, 2015, pp. 3262-3274.
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